{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Kearneysville",
      "state": "WV",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79968",
      "recalling_firm": "Randox Laboratories",
      "address_1": "515 Industrial Blvd",
      "address_2": "N/A",
      "postal_code": "25430-2778",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Distribution including Puerto Rico and the state of : West Virginia.",
      "recall_number": "Z-2059-2018",
      "product_description": "RX Imola (RX4900)    For Professional Use for the quantitative in vitro determination of various clinical chemistry tests.",
      "product_quantity": "41  analyzers",
      "reason_for_recall": "Abnormal premature termination of the software could affect the use of the analyser when running patient samples. The impact being a delay in reporting test results.",
      "recall_initiation_date": "20180504",
      "center_classification_date": "20180604",
      "termination_date": "20200616",
      "report_date": "20180613",
      "code_info": "GTIN 05055273206104. All serial numbers."
    }
  ]
}